400890
cis-2-Butene
≥99%
Synonym(s):
(2Z)-2-Butene, (Z)-2-Butene, Z-Butene, cis-1,2-Dimethylethylene, cis-2-Butylene
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About This Item
Linear Formula:
CH3CH=CHCH3
CAS Number:
Molecular Weight:
56.11
Beilstein:
1361341
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
vapor density
2 (vs air)
Quality Level
vapor pressure
1414 mmHg ( 21 °C)
Assay
≥99%
form
gas
autoignition temp.
615 °F
expl. lim.
9.7 %
bp
3.7 °C (lit.)
mp
−139 °C (lit.)
SMILES string
[H]\C(C)=C(/[H])C
InChI
1S/C4H8/c1-3-4-2/h3-4H,1-2H3/b4-3-
InChI key
IAQRGUVFOMOMEM-ARJAWSKDSA-N
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Application
cis-2-Butene is an unsaturated olefinic hydrocarbon used as a precursor in the polymerization of gasoline. It is also used to synthesize butadiene and other aliphatic C4/C5 organic molecules. It is also employed as a cross-linking agent.
Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
Storage Class Code
2A - Gases
WGK
WGK 3
Flash Point(F)
10.4 °F - closed cup
Flash Point(C)
-12 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Basic organic chemicals
Polymer, 117-141 (2002)
Competition and miscibility of isodimorphism and their effects on band spherulites and mechanical properties of poly (butylene succinate-co-cis-butene succinate) unsaturated aliphatic copolyesters
Yu Y, et al.
Polymer, 150, 52-63 (2018)
J T Groves et al.
Progress in clinical and biological research, 274, 509-524 (1988-01-01)
A cytochrome P-450 LM2 reconstituted system mediated expoxidations of small terminal alkenes to the corresponding alkyloxiranes. This oxidation was accompanied by a stereoselective proton exchange of the E proton. Propene was oxidized in D2O to trans-3-deuterio-2-methyloxirane, and E-1-deuteriopropene was epoxidized
Philip T M Carlsson et al.
Physical chemistry chemical physics : PCCP, 14(45), 15637-15640 (2012-10-24)
Recent studies have suggested that the reaction of stabilised Criegee Intermediates (CIs) with sulfur dioxide (SO(2)), leading to the formation of a carbonyl compound and sulfur trioxide, is a relevant atmospheric source of sulfuric acid. Here, the significance of this
Duangkamol Gleeson
Journal of computer-aided molecular design, 22(8), 579-585 (2008-03-18)
In this study the results from a series of calculations are reported that probe the influence of the QM cluster size and the extended framework treatment in ONIOM calculations. This is done by comparing the differences in the structures and
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